WO2007017291A2 - Realisation d'une solution d'oxaliplatine et contenant et jeu de contenants avec cette solution - Google Patents

Realisation d'une solution d'oxaliplatine et contenant et jeu de contenants avec cette solution Download PDF

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Publication number
WO2007017291A2
WO2007017291A2 PCT/EP2006/007982 EP2006007982W WO2007017291A2 WO 2007017291 A2 WO2007017291 A2 WO 2007017291A2 EP 2006007982 W EP2006007982 W EP 2006007982W WO 2007017291 A2 WO2007017291 A2 WO 2007017291A2
Authority
WO
WIPO (PCT)
Prior art keywords
oxaliplatin
acid
solution
concentration
container
Prior art date
Application number
PCT/EP2006/007982
Other languages
German (de)
English (en)
Other versions
WO2007017291A3 (fr
Inventor
Michaela Roth
Katrin MEYER-WÜLFING
Original Assignee
Hexal Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hexal Ag filed Critical Hexal Ag
Priority to US12/063,531 priority Critical patent/US20100140131A1/en
Priority to EP06776798A priority patent/EP1916996A2/fr
Publication of WO2007017291A2 publication Critical patent/WO2007017291A2/fr
Publication of WO2007017291A3 publication Critical patent/WO2007017291A3/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/28Compounds containing heavy metals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/28Compounds containing heavy metals
    • A61K31/282Platinum compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/555Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/12Carboxylic acids; Salts or anhydrides thereof

Definitions

  • EP 0 943 331 B1 describes a stable oxaliplatin solution with oxalic acid or an oxalic acid salt as buffer.
  • the solution can be filled into an ampoule, glass vial (page 8, line 10), infusion bag or syringe. Disadvantage of this formulation is a certain toxicity of oxalic acid.
  • WO 03/047 587 discloses a stable oxaliplatin solution in suitable containers (page 12, line 28) with lactic acid or a lactic acid salt as buffer.
  • the present invention relates to the use of an acid to increase the solubility of oxaliplatin in an aqueous solution.
  • the invention relates to a process for the preparation of an aqueous oxaliplatin solution in which oxaliplatinol is dissolved in water by adding an acid to an oxaliplatin concentration which increases over an acid-free aqueous oxaliplatin solution, in particular under otherwise identical conditions is.
  • the present invention relates to a process for the preparation of a solution consisting of oxaliplatin, an acid and water, in which oxaliplatin is dissolved in water by adding an acid to an oxaliplatin concentration which is elevated over an acid-free aqueous oxaliplatin solution.
  • oxaliplatin in the method of the present invention, can be dissolved in water by adding the acid to the highest oxaliplatin saturation concentration achievable with this acid.
  • an oxaliplatin concentration which is in the range which is determined on the one hand by the saturation concentration of an acid-free aqueous oxaliplatin solution and on the other hand by the highest saturation concentration in the presence of the acid is defined and the acid is added until the predetermined concentration is reached.
  • the solution is free from carbohydrate such as e.g. Lactose, glucose, maltose, fructose, galactose or dextrans (e.g., 10-70).
  • carbohydrate such as e.g. Lactose, glucose, maltose, fructose, galactose or dextrans (e.g., 10-70).
  • the solution is free of polyethylene glycol, e.g. Polyethylene glycol 200, 300, 400 and 600 added.
  • an integer or half-integer (integer plus 1) oxaliplatin concentration of a customary concentration unit of measure preferably the unit of measure mg / ml or molar.
  • an inorganic and / or organic acid can be used in the process according to the invention.
  • At least one inorganic acid can be used from the group formed by sulfuric acid, nitric acid and phosphoric acid.
  • sulfuric acid is used.
  • At least one organic acid may be used from the group formed by citric acid, succinic acid, ascorbic acid, oxalic acid, lactic acid and malonic acid.
  • Citric acid is preferably used.
  • a buffering salt Furthermore, in the method according to the invention, it is additionally possible to use a buffering salt. Furthermore, in the method according to the invention, a pH of 1 to 7 and in particular 1.5 to 4 can be set.
  • the container can be closed under an inert gas.
  • a vial, a screw-cap bottle or an ampoule can be provided as a container.
  • a vial as a bottle, which is designed as a single-dose or multi-dose container.
  • Another embodiment of the invention relates to a container of aqueous oxaliplatin solution obtainable by the process according to the invention.
  • Another embodiment of the invention relates to a container having an acidic oxaliplatin aqueous solution of an oxaliplatin concentration which is elevated relative to an acid-free oxaliplatin aqueous solution.
  • a further embodiment of the invention relates to a container with an acidic aqueous oxaliplatin solution with the highest oxaliplatin saturation concentration, which is achievable with the aid of this acid, or with the highest for the acid characteristic oxaliplatin saturation concentration.
  • a further embodiment of the invention relates to a container with an acidic aqueous oxaliplatin solution having an integer or half integer (integer plus M) oxaliplatin concentration of a conventional concentration unit, preferably the unit mg oxaliplatin / ml solution or mg oxaliplatin / mg solution or molar.
  • a further embodiment of the invention relates to a set of or containers according to the invention each having an acidic oxaliplatin aqueous solution having an integer or integer (integer plus M) oxaliplatin concentration of a conventional concentration unit, preferably mg oxaliplatin / ml Solution or mg oxaliplatin / mg solution or molar.
  • an embodiment of the invention relates to a set of or containers according to the invention each having an acidic aqueous oxaliplatin solution with an integer or half integer (integer plus M) oxaliplatin concentration of a conventional concentration unit, preferably the unit mg oxaliplatin / ml Solution or mg oxaliplatin / mg solution or molar, whereby the oxaliplatin concentration of at least one container deviates from the concentration of the other container (s).
  • the present invention further comprises the solutions prepared according to one of the described methods.
  • 5 examples are used to tabulate the increased oxaliplatin solubility in the presence of acid.

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne un procédé pour réaliser une solution aqueuse d'oxaliplatine, selon lequel de d'oxaliplatine est dissoute dans de l'eau par ajout d'un acide jusqu'à l'obtention d'une concentration d'oxaliplatine supérieure à celle d'une solution aqueuse d'oxaliplatine sans acide. La présente invention porte également sur un contenant et un jeu de contenants avec cette solution.
PCT/EP2006/007982 2005-08-11 2006-08-11 Realisation d'une solution d'oxaliplatine et contenant et jeu de contenants avec cette solution WO2007017291A2 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US12/063,531 US20100140131A1 (en) 2005-08-11 2006-08-11 Production of an Oxaliplatin Mixture and a Container and a Container Set for Said Mixture
EP06776798A EP1916996A2 (fr) 2005-08-11 2006-08-11 Realisation d'une solution d'oxaliplatine et contenant et jeu de contenants avec cette solution

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005038347A DE102005038347A1 (de) 2005-08-11 2005-08-11 Herstellung einer Oxaliplatin-Lösung und Behälter sowie Behälter-Set mit der Lösung
DE102005038347.5 2005-08-11

Publications (2)

Publication Number Publication Date
WO2007017291A2 true WO2007017291A2 (fr) 2007-02-15
WO2007017291A3 WO2007017291A3 (fr) 2007-05-24

Family

ID=37179055

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2006/007982 WO2007017291A2 (fr) 2005-08-11 2006-08-11 Realisation d'une solution d'oxaliplatine et contenant et jeu de contenants avec cette solution

Country Status (4)

Country Link
US (1) US20100140131A1 (fr)
EP (1) EP1916996A2 (fr)
DE (1) DE102005038347A1 (fr)
WO (1) WO2007017291A2 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5929607B2 (ja) * 2012-08-06 2016-06-08 ニプロ株式会社 オキサリプラチン製剤

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999043355A2 (fr) * 1998-02-25 1999-09-02 Sanofi-Synthelabo Formulations
US6476068B1 (en) * 2001-12-06 2002-11-05 Pharmacia Italia, S.P.A. Platinum derivative pharmaceutical formulations
EP1466600A1 (fr) * 2003-03-28 2004-10-13 Stada Arzneimittel Ag Solutions d'oxaliplatine prêtes à l'emploi
WO2005020980A1 (fr) * 2003-08-28 2005-03-10 Mayne Pharma Pty Ltd Formulations d'oxaliplatine contenant de l'acide
DE102004063764A1 (de) * 2004-12-29 2006-07-13 Hexal Ag Kunststoff-Flasche für Oxaliplatin

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2002223013A1 (en) * 2000-12-12 2002-06-24 Debiopharm S.A. Pharmaceutical oxaliplatinum preparation for parenteral administration and method for obtaining same
CA2357955C (fr) * 2001-09-28 2008-11-18 Itf Technologies Optiques Inc./Itf Optical Technologies Inc. Depolariseur tout fibre optique
US20060063833A1 (en) * 2004-09-22 2006-03-23 Edgar Schridde Ready-to-use oxaliplatin solutions
DE102004052877B4 (de) * 2004-11-02 2008-06-19 Ebewe Pharma Ges.M.B.H. Nfg.Kg Stabile wässrige Formulierungen eines Platin-Derivats

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999043355A2 (fr) * 1998-02-25 1999-09-02 Sanofi-Synthelabo Formulations
US6476068B1 (en) * 2001-12-06 2002-11-05 Pharmacia Italia, S.P.A. Platinum derivative pharmaceutical formulations
US20030109515A1 (en) * 2001-12-06 2003-06-12 Pharmacia Italia, Spa. Pharmaceutical formulation of a platinum derivative
EP1466600A1 (fr) * 2003-03-28 2004-10-13 Stada Arzneimittel Ag Solutions d'oxaliplatine prêtes à l'emploi
WO2005020980A1 (fr) * 2003-08-28 2005-03-10 Mayne Pharma Pty Ltd Formulations d'oxaliplatine contenant de l'acide
DE102004063764A1 (de) * 2004-12-29 2006-07-13 Hexal Ag Kunststoff-Flasche für Oxaliplatin

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1916996A2 *

Also Published As

Publication number Publication date
US20100140131A1 (en) 2010-06-10
EP1916996A2 (fr) 2008-05-07
DE102005038347A1 (de) 2007-02-15
WO2007017291A3 (fr) 2007-05-24

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